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Variant : CV82321 (NM_152591.2(CCDC63):c.1078G>A (p.Glu360Lys)) Homo sapiens

Symbol: CV82321
Name: NM_152591.2(CCDC63):c.1078G>A (p.Glu360Lys)
Condition: Malignant melanoma [RCV000062400]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: CCDC63  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000012.10:g.109815266G>A
NC_000012.12:g.110893079G>A
NC_000012.11:g.111330883G>A
NM_152591.2:c.1078G>A
NM_152591.1:c.1078G>A
NP_689804.1:p.Glu360Lys
Position
Human AssemblyChrPosition (strand)Source
GRCh3812110,893,079 - 110,893,079CLINVAR
GRCh3712111,330,883 - 111,330,883CLINVAR
Build 3612109,815,266 - 109,815,266CLINVAR
Cytogenetic Map1212q24.11CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8627177
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.